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Mam, dou have any PPT regarding molecular biology, plz answer

Thank you

thank you

Very helpful thank you so much

Straight to the point better than my instructor 😅

Wow, that really helps alot. I don't think I need a education for that.

Thank you very much. your video is really easy to understand and helpful for me. Keep it up dear

Thanks a lot for making such short and too precise video. 🫶

Thanks for the help! I have a microscope myself and this video really helped me with the glass slides.

I’m not sure if we’re supposed to be able to hear but halfway through the video the audio stops playing I can’t hear anything

Wonderful video! I will caution students and researchers that one of these "rules" is often broken. In scientific publications and software, two "paired" strands are often written together (one above the other), but *without* the 5'/3' labels. This makes it very easy to forget that the bottom strand is actually 3' → 5' and can result in confusion and accidental propagation of "reverse" sequence (without realizing it). So I recommend that you imagine the 5' / 3' label on the top strand and the 3' / 5' labels on the bottom strand to avoid confusion. Also, when copying/pasting sequence info, use the top strand as much as possible (and use software to generate the reverse-complement as needed).

LEGEND!

Thanks sir for making it clear 🙏🏼🔥

Interesting procedure but that egg under the microscope at the end will make me cringe every time. - CM

Thank you, I was so confused about this thing 😢 thanks

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Thank you so much,the thing is i use to write it in wrong way because i don't flip the sequence and my teacher does not clear that thank you

OMG THIS MAKES MY LIFE MUCH MORE EASIER!!! THANK U VERY MUCH

Great video! I have my first micro quiz tomorrow and you’ve absolutely helped. Thank you.

If the CFU on the plates are all outside the greater than 30 but less than 300 range, do you have to redo the serial dilution?

One of the clearest and most concise explanations. Thank You!

I am getting lost in the calculation. Would please make more samples of calculations?

Thank you very much very informative video. kindly tell me how to pack culture of nitrifying bacteria in sashay or a bottle actually i am asking about the media some people pack bacteria in powder form how they do it?

Miss can you tell me the direction of these sequence CTGACG

What is the last thing you applied to the plates?

you deserved my subscription.. i love them, clear and compact. good job

Would i be able to send you some pictures of my colonies in order to help identify them?

From colony morphology can we identify the bacteria name?

Great video Ms.Brunings!! Personally, I found this activity fun And interesting. Keep up the hard work. 👍👍 Don’t forget to add friends. 😂😂

Lol Asha! I have two dogs. I feel like the UV light is going to be well used even after this At-Home lab.

Great job professor

Great Video